美国药品NDC(国家药品编码)与药品说明书数据库(U.S. FDA National Drug Code DataBase)
检索条件:" 注册申请号=ANDA077095"
NDC包装代码 产品NDC 产品类型 商品名 通用名 剂型 给药途径 上市日期 结束日期 市场类别 申请号 标签持有者 活性成分 规格 包装描述
71610-920-53 71610-920 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20250701 N/A ANDA ANDA077095 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 500 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71610-920-53)
71610-920-60 71610-920 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20250701 N/A ANDA ANDA077095 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 500 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71610-920-60)
71610-920-80 71610-920 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20250701 N/A ANDA ANDA077095 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 500 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71610-920-80)
71610-929-30 71610-929 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20250722 N/A ANDA ANDA077095 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 500 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71610-929-30)
71610-929-53 71610-929 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20250722 N/A ANDA ANDA077095 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 500 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71610-929-53)
71610-929-60 71610-929 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20250722 N/A ANDA ANDA077095 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 500 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71610-929-60)
71610-929-70 71610-929 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20250722 N/A ANDA ANDA077095 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 500 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71610-929-70)
71610-929-80 71610-929 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20250722 N/A ANDA ANDA077095 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 500 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71610-929-80)
71610-929-94 71610-929 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20250722 N/A ANDA ANDA077095 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 500 mg/1 360 TABLET, FILM COATED in 1 BOTTLE (71610-929-94)
71610-941-60 71610-941 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20250825 N/A ANDA ANDA077095 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 1000 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71610-941-60)
71610-941-80 71610-941 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20250825 N/A ANDA ANDA077095 Aphena Pharma Solutions - Tennessee, LLC METFORMIN HYDROCHLORIDE 1000 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71610-941-80)
50090-7868-0 50090-7868 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20260129 N/A ANDA ANDA077095 A-S Medication Solutions METFORMIN HYDROCHLORIDE 1000 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-7868-0)
65862-008-90 65862-008 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20050114 N/A ANDA ANDA077095 Aurobindo Pharma Limited METFORMIN HYDROCHLORIDE 500 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65862-008-90)
65862-008-99 65862-008 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20050114 N/A ANDA ANDA077095 Aurobindo Pharma Limited METFORMIN HYDROCHLORIDE 500 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-008-99)
65862-008-01 65862-008 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20050114 N/A ANDA ANDA077095 Aurobindo Pharma Limited METFORMIN HYDROCHLORIDE 500 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-008-01)
65862-008-05 65862-008 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20050114 N/A ANDA ANDA077095 Aurobindo Pharma Limited METFORMIN HYDROCHLORIDE 500 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-008-05)
65862-008-33 65862-008 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20050114 N/A ANDA ANDA077095 Aurobindo Pharma Limited METFORMIN HYDROCHLORIDE 500 mg/1 300 TABLET, FILM COATED in 1 BOTTLE (65862-008-33)
65862-008-45 65862-008 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20050114 N/A ANDA ANDA077095 Aurobindo Pharma Limited METFORMIN HYDROCHLORIDE 500 mg/1 4500 TABLET, FILM COATED in 1 BOTTLE (65862-008-45)
65862-008-50 65862-008 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20050114 N/A ANDA ANDA077095 Aurobindo Pharma Limited METFORMIN HYDROCHLORIDE 500 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (65862-008-50)
65862-008-60 65862-008 HUMAN PRESCRIPTION DRUG Metformin Hydrochloride Metformin Hydrochloride TABLET, FILM COATED ORAL 20050114 N/A ANDA ANDA077095 Aurobindo Pharma Limited METFORMIN HYDROCHLORIDE 500 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65862-008-60)
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